1-3 of 3
Jonathan T. Wilde
Close
Sort by
Journal Articles

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

Brief Report
Jacqueline Stockley, Neil V. Morgan, Danai Bem, Gillian C. Lowe, Marie Lordkipanidzé, Ban Dawood, Michael A. Simpson, Kirsty Macfarlane, Kevin Horner, Vincenzo C. Leo, Katherine Talks, Jayashree Motwani, Jonathan T. Wilde, Peter W. Collins, Michael Makris, Steve P. Watson, Martina E. Daly
Journal: Blood
Blood (2013) 122 (25): 4090–4093.
https://doi.org/10.1182/blood-2013-06-506873
Published: 2013
Includes: Supplemental data
Journal Articles

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Clinical Trials & Observations
Ban B. Dawood, Gillian C. Lowe, Marie Lordkipanidzé, Danai Bem, Martina E. Daly, Mike Makris, Andrew Mumford, Jonathan T. Wilde, Steve P. Watson
Journal: Blood
Blood (2012) 120 (25): 5041–5049.
https://doi.org/10.1182/blood-2012-07-444281
Published: 2012
Includes: Supplemental data
Journal Articles

Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

Brief Report
Martina E. Daly, Ban B. Dawood, William A. Lester, Ian R. Peake, Francesco Rodeghiero, Anne C. Goodeve, Michael Makris, Jonathan T. Wilde, Andrew D. Mumford, Stephen P. Watson, Stuart J. Mundell
Journal: Blood
Blood (2009) 113 (17): 4110–4113.
https://doi.org/10.1182/blood-2008-11-190850
Published: 2009